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Spinocerebellar ataxia type 15/16
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Spinocerebellar ataxia type 15/16
Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency

ITPR1
(UniProt - OMIM)
 GRM1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ITPR1
(0.52)
GRM1


Citations in the biomedical literature:


Spinocerebellar ataxia type 15/16
ITPR1
Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency
GRM1



Spinocerebellar ataxia type 15/16
Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency

Synonym(s):
- SCA15/16
Synonym(s):
- Autosomal recessive congenital cerebellar ataxia due to metabotropic glutamate receptor 1 deficiency
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.